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109 related items for PubMed ID: 17099166

  • 1. Rosenthal fiber encephalopathy in a dog resembling Alexander disease in humans.
    Alemañ N, Marcaccini A, Espino L, Bermúdez R, Nieto JM, López-Peña M.
    Vet Pathol; 2006 Nov; 43(6):1025-8. PubMed ID: 17099166
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  • 2. Alexander's disease in a Bernese mountain dog.
    Weissenböck H, Obermaier G, Dahme E.
    Acta Neuropathol; 1996 Nov; 91(2):200-4. PubMed ID: 8787155
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  • 3. A Rosenthal fiber encephalomyelopathy resembling Alexander's disease in 3 sheep.
    Kessell AE, Finnie JW, Manavis J, Cheetham GD, Blumbergs PC.
    Vet Pathol; 2012 Mar; 49(2):248-54. PubMed ID: 21233330
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  • 4. Mild functional effects of a novel GFAP mutant allele identified in a familial case of adult-onset Alexander disease.
    Bachetti T, Caroli F, Bocca P, Prigione I, Balbi P, Biancheri R, Filocamo M, Mariotti C, Pareyson D, Ravazzolo R, Ceccherini I.
    Eur J Hum Genet; 2008 Apr; 16(4):462-70. PubMed ID: 18197187
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  • 5. The origin of Rosenthal fibers and their contributions to astrocyte pathology in Alexander disease.
    Sosunov AA, McKhann GM, Goldman JE.
    Acta Neuropathol Commun; 2017 Mar 31; 5(1):27. PubMed ID: 28359321
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  • 6. Murine model of Alexander disease: analysis of GFAP aggregate formation and its pathological significance.
    Tanaka KF, Takebayashi H, Yamazaki Y, Ono K, Naruse M, Iwasato T, Itohara S, Kato H, Ikenaka K.
    Glia; 2007 Apr 15; 55(6):617-31. PubMed ID: 17299771
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  • 7. Synemin is expressed in reactive astrocytes and Rosenthal fibers in Alexander disease.
    Pekny T, Faiz M, Wilhelmsson U, Curtis MA, Matej R, Skalli O, Pekny M.
    APMIS; 2014 Jan 15; 122(1):76-80. PubMed ID: 23594359
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  • 8. The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27.
    Der Perng M, Su M, Wen SF, Li R, Gibbon T, Prescott AR, Brenner M, Quinlan RA.
    Am J Hum Genet; 2006 Aug 15; 79(2):197-213. PubMed ID: 16826512
    [Abstract] [Full Text] [Related]

  • 9. Novel deletion mutation in GFAP gene in an infantile form of Alexander disease.
    Murakami N, Tsuchiya T, Kanazawa N, Tsujino S, Nagai T.
    Pediatr Neurol; 2008 Jan 15; 38(1):50-2. PubMed ID: 18054694
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  • 12. Fluoro-Jade: new fluorescent marker of Rosenthal fibers.
    Tanaka KF, Ochi N, Hayashi T, Ikeda E, Ikenaka K.
    Neurosci Lett; 2006 Oct 23; 407(2):127-30. PubMed ID: 16949206
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  • 13. Beneficial effects of curcumin on GFAP filament organization and down-regulation of GFAP expression in an in vitro model of Alexander disease.
    Bachetti T, Di Zanni E, Balbi P, Ravazzolo R, Sechi G, Ceccherini I.
    Exp Cell Res; 2012 Sep 10; 318(15):1844-54. PubMed ID: 22705585
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  • 14. Review of Alexander disease: beyond the classical concept of leukodystrophy.
    Sawaishi Y.
    Brain Dev; 2009 Aug 10; 31(7):493-8. PubMed ID: 19386454
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  • 17. Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease.
    Li R, Johnson AB, Salomons G, Goldman JE, Naidu S, Quinlan R, Cree B, Ruyle SZ, Banwell B, D'Hooghe M, Siebert JR, Rolf CM, Cox H, Reddy A, Gutiérrez-Solana LG, Collins A, Weller RO, Messing A, van der Knaap MS, Brenner M.
    Ann Neurol; 2005 Mar 10; 57(3):310-26. PubMed ID: 15732097
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  • 18. Alexander's disease: a case report of a biopsy proven case.
    Tatke M, Sharma A.
    Neurol India; 1999 Dec 10; 47(4):333-5. PubMed ID: 10625914
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  • 19. Clinical and genetic study in Chinese patients with Alexander disease.
    Ye Wu, Qiang Gu, Jingmin Wang, Yanling Yang, Xiru Wu, Yuwu Jiang.
    J Child Neurol; 2008 Feb 10; 23(2):173-7. PubMed ID: 18079314
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  • 20. Lithium Decreases Glial Fibrillary Acidic Protein in a Mouse Model of Alexander Disease.
    LaPash Daniels CM, Paffenroth E, Austin EV, Glebov K, Lewis D, Walter J, Messing A.
    PLoS One; 2015 Feb 10; 10(9):e0138132. PubMed ID: 26378915
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